A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5997384



Internal ID21906727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27462894..27469616hg38UCSC Ensembl
chr4:27464516..27471238hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg386723
hg196723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5997384
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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